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rs137853104

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs137853104(A;A)
Make rs137853104(A;G)
ReferenceGRCh38 38.1/141
Chromosome12
Position53429907
GeneAMHR2
is asnp
is mentioned by
dbSNPrs137853104
ebirs137853104
HLIrs137853104
Exacrs137853104
Varsomers137853104
Maprs137853104
PheGenIrs137853104
hapmaprs137853104
1000 genomesrs137853104
hgdprs137853104
ensemblrs137853104
gopubmedrs137853104
geneviewrs137853104
scholarrs137853104
googlers137853104
pharmgkbrs137853104
gwascentralrs137853104
openSNPrs137853104
23andMers137853104
23andMe allrs137853104
SNP Nexus

SNPshotrs137853104
SNPdbers137853104
MSV3drs137853104
GWAS Ctlgrs137853104
Max Magnitude0
OMIM600956
Desc
Variant0004
Relatedalso
ClinVar
Risk rs137853104(A;A)
Alt rs137853104(A;A)
Reference rs137853104(G;G)
Significance Pathogenic
Disease Persistent mullerian duct syndrome
Variation info
Gene AMHR2
CLNDBN Persistent mullerian duct syndrome, type II
Reversed 0
HGVS NC_000012.11:g.53823691G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000009161.2,